Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Abdelbary, Ghada A."'
Autor:
AbuBakr, Abdel-Hameed, Hassan, Hatem A.F.M., Abdalla, Ahmed, Khowessah, Omneya M., Abdelbary, Ghada A.
Publikováno v:
In International Journal of Pharmaceutics 25 March 2023 635
Publikováno v:
In Journal of Drug Delivery Science and Technology June 2020 57
Publikováno v:
In Journal of Drug Delivery Science and Technology February 2019 49:603-614
Publikováno v:
In Journal of Drug Delivery Science and Technology February 2018 43:253-261
Publikováno v:
In Journal of Drug Delivery Science and Technology June 2016 33:98-113
Publikováno v:
In European Journal of Pharmaceutics and Biopharmaceutics February 2014 86(2):178-189
Autor:
Abd El-Halim, Shady M.1 (AUTHOR) shady_mohammed@o6u.edu.eg, Abdelbary, Ghada A.2 (AUTHOR), Amin, Maha M.2 (AUTHOR), Zakaria, Mohamed Y.3 (AUTHOR), Shamsel-Din, Hesham A.4 (AUTHOR), Ibrahim, Ahmed B.4 (AUTHOR)
Publikováno v:
DARU: Journal of Pharmaceutical Sciences. 6/20/2020, Vol. 28, p517-532. 16p.
Publikováno v:
In International Journal of Pharmaceutics 16 August 2013 452(1-2):300-310
Autor:
Abdelbary, Ghada, Nebsen, Marianne
Publikováno v:
In Journal of Pharmacy Research January 2013 7(1):24-32
Autor:
Nekouian Reza, Xing Chang-Yang, Abdelbary Ghada, Abdelmahmoud Abdelkarim Maki Marwan, Amir Yasin Ahmadi Seyyed, H. Teaima Mahmoud, Elumalai Manogaran, Ansari-moghaddam Bijan, Li Zhelong, Sun Wenqi, Yang Guodong, M. El-Mahrouk Galal, Shahsavar Farhad, Daduang Jureerut, Mousavi Nazanin, Panpitakkul Panjaree, Priprem Aroonsri, Sangchart Pimpitchaya, Somudorn Jirachaya, Bayazeid Omer, Mahakunakorn Pramote, A. Hakeem Eman, Mahmoudi Zahra, Vijayaraj Kumar Palanirajan, Damrongrungruang Teerasak, Zhou Xueying, Uthaiwat Prangtip, Yuan Lijun, Puthongking Ploenthip, Panyatip Panyada
Publikováno v:
Current Pharmacogenomics and Personalized Medicine. 17:94-103
Objectives: OXP3 is a gene related to regulatory T cells existing on chromosome X. This meta-analysis, based on genetic association studies, was conducted to investigate the association of FOXP3 polymorphisms with susceptibility to multiple sclerosis